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Examples of path functions include work, heat and arc length. In contrast to path functions, state functions are independent of the path taken. Thermodynamic state variables are point functions, differing from path functions. For a given state, considered as a point, there is a definite value for each state variable and state function.
The difference between initial and final states of the system's internal energy does not account for the extent of the energy interactions transpired. Therefore, internal energy is a state function (i.e. exact differential), while heat and work are path functions (i.e. inexact differentials) because integration must account for the path taken.
In the thermodynamics of equilibrium, a state function, function of state, or point function for a thermodynamic system is a mathematical function relating several state variables or state quantities (that describe equilibrium states of a system) that depend only on the current equilibrium thermodynamic state of the system [1] (e.g. gas, liquid, solid, crystal, or emulsion), not the path which ...
This Process Path is a straight horizontal line from state one to state two on a P-V diagram. Figure 2. It is often valuable to calculate the work done in a process. The work done in a process is the area beneath the process path on a P-V diagram. Figure 2 If the process is isobaric, then the work done on the piston is easily calculated.
Thermodynamic temperature is a specifically thermodynamic concept, while the original directly measureable state variables are defined by ordinary physical measurements, without reference to thermodynamic concepts; for this reason, it is helpful to regard thermodynamic temperature as a state function.
An example of a cycle of idealized thermodynamic processes which make up the Stirling cycle. A quasi-static thermodynamic process can be visualized by graphically plotting the path of idealized changes to the system's state variables. In the example, a cycle consisting of four quasi-static processes is shown.
The concepts of Hess's law can be expanded to include changes in entropy and in Gibbs free energy, since these are also state functions. The Bordwell thermodynamic cycle is an example of such an extension that takes advantage of easily measured equilibria and redox potentials to determine experimentally inaccessible Gibbs free energy values.
Heat transfer is a process function (or path function), as opposed to functions of state; therefore, the amount of heat transferred in a thermodynamic process that changes the state of a system depends on how that process occurs, not only the net difference between the initial and final states of the process.